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FDA Inspection
•Eurofins Biopharma Product Testing Sweden AB•June 27, 2019

Eurofins Biopharma Product Testing Sweden AB – FDA Inspection, Jun 27, 2019

Record Details

This FDA Inspection record concerns Eurofins Biopharma Product Testing Sweden AB, with an inspection on June 27, 2019, issued by the Center for Veterinary Medicine, covering veterinary.

Company
Eurofins Biopharma Product Testing Sweden AB
Inspection Date
June 27, 2019
Product Type
Veterinary
Office
Center for Veterinary Medicine
Person
  • Ileana Barreto-Pettit (Issuing Officer)
View Company Profile

ID · f5c45727-89ef-45e2-80c9-7e6e4e73df07

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1096830
FDA center
Animal Drugs & Feeds
Project area
Monitoring of Marketed Animal Drugs, Feed, and Devices

Other FDA inspections of Eurofins Biopharma Product Testing Sweden AB

3
DateClassificationOfficeProject area
June 19, 2024VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 9, 2015NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
February 16, 2011VAICenter for Veterinary MedicinePre-Approval Eval. of Animal Drugs and Food Additives
Other documents for Eurofins Biopharma Product Testing Sweden AB
  • FDA Inspection 1273937 - 2024-06-19
  • FDA Inspection 920664 - 2015-03-09
  • FDA Inspection 725045 - 2011-02-16

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